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Previous release (v1)
2025-01-31 08:36:31, GGRNA.v2 : RefSeq release 227 (Nov, 2024)
LOCUS NM_001284408 1797 bp mRNA linear PRI 08-JUN-2024
DEFINITION Homo sapiens transmembrane protein 40 (TMEM40), transcript variant
4, mRNA.
ACCESSION NM_001284408 XM_005265309
VERSION NM_001284408.2
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 1797)
AUTHORS Lim,S.H., Snider,J., Birimberg-Schwartz,L., Ip,W., Serralha,J.C.,
Botelho,H.M., Lopes-Pacheco,M., Pinto,M.C., Moutaoufik,M.T.,
Zilocchi,M., Laselva,O., Esmaeili,M., Kotlyar,M., Lyakisheva,A.,
Tang,P., Lopez Vazquez,L., Akula,I., Aboualizadeh,F., Wong,V.,
Grozavu,I., Opacak-Bernardi,T., Yao,Z., Mendoza,M., Babu,M.,
Jurisica,I., Gonska,T., Bear,C.E., Amaral,M.D. and Stagljar,I.
TITLE CFTR interactome mapping using the mammalian membrane two-hybrid
high-throughput screening system
JOURNAL Mol Syst Biol 18 (2), e10629 (2022)
PUBMED 35156780
REFERENCE 2 (bases 1 to 1797)
AUTHORS Zhang,Q., Huang,D., Zhang,Z., Feng,Y., Fu,M., Wei,M., Zhou,J.,
Huang,Y., Liu,S. and Shi,R.
TITLE High expression of TMEM40 contributes to progressive features of
tongue squamous cell carcinoma
JOURNAL Oncol Rep 41 (1), 154-164 (2019)
PUBMED 30320346
REMARK GeneRIF: Study found that TMEM40 expression was increased in tongue
squamous cell carcinoma (TSCC) tissues and associated with
clinicopathological parameters. Further results indicated that
TMEM40 promoted TSCC development and progression via regulation of
p53, Bax and MMP9.
REFERENCE 3 (bases 1 to 1797)
AUTHORS Zhang,Z.F., Zhang,H.R., Zhang,Q.Y., Lai,S.Y., Feng,Y.Z., Zhou,Y.,
Zheng,S.R., Shi,R. and Zhou,J.Y.
TITLE High expression of TMEM40 is associated with the malignant behavior
and tumorigenesis in bladder cancer
JOURNAL J Transl Med 16 (1), 9 (2018)
PUBMED 29351801
REMARK GeneRIF: TMEM40 represents a potential oncogene, which exert a
crucial role in the proliferation and apoptosis via the p53
signaling pathway in bladder cancer.
Publication Status: Online-Only
REFERENCE 4 (bases 1 to 1797)
AUTHORS Pankow,S., Bamberger,C., Calzolari,D., Martinez-Bartolome,S.,
Lavallee-Adam,M., Balch,W.E. and Yates,J.R. 3rd.
TITLE F508 CFTR interactome remodelling promotes rescue of cystic
fibrosis
JOURNAL Nature 528 (7583), 510-516 (2015)
PUBMED 26618866
REFERENCE 5 (bases 1 to 1797)
AUTHORS Macaulay,I.C., Tijssen,M.R., Thijssen-Timmer,D.C., Gusnanto,A.,
Steward,M., Burns,P., Langford,C.F., Ellis,P.D., Dudbridge,F.,
Zwaginga,J.J., Watkins,N.A., van der Schoot,C.E. and Ouwehand,W.H.
TITLE Comparative gene expression profiling of in vitro differentiated
megakaryocytes and erythroblasts identifies novel activatory and
inhibitory platelet membrane proteins
JOURNAL Blood 109 (8), 3260-3269 (2007)
PUBMED 17192395
REFERENCE 6 (bases 1 to 1797)
AUTHORS Gevaert,K., Goethals,M., Martens,L., Van Damme,J., Staes,A.,
Thomas,G.R. and Vandekerckhove,J.
TITLE Exploring proteomes and analyzing protein processing by mass
spectrometric identification of sorted N-terminal peptides
JOURNAL Nat Biotechnol 21 (5), 566-569 (2003)
PUBMED 12665801
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AK092470.1, BG335433.1, AK001898.1, AI452552.1 and AC034198.7.
On Jun 1, 2019 this sequence version replaced NM_001284408.1.
Transcript Variant: This variant (4) differs in the 5' UTR, lacks a
portion of the 5' coding region, initiates translation at a
downstream in-frame start codon, and lacks two alternate in-frame
exons in the central coding region, compared to variant 1. The
encoded isoform (d) is shorter at the N-terminus, compared to
isoform a.
##Evidence-Data-START##
Transcript exon combination :: SRR7346977.583357.1,
SRR7346977.428566.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA2142853 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-11 AK092470.1 51-61
12-583 BG335433.1 1-572
584-1132 AK001898.1 704-1252
1133-1432 AK092470.1 1411-1710
1433-1795 AI452552.1 5-367 c
1796-1797 AC034198.7 147822-147823
FEATURES Location/Qualifiers
source 1..1797
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="3"
/map="3p25.2"
gene 1..1797
/gene="TMEM40"
/note="transmembrane protein 40"
/db_xref="GeneID:55287"
/db_xref="HGNC:HGNC:25620"
exon 1..69
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 3
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:898442973"
variation 6
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:545756764"
variation 8
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:995604096"
variation 10
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:548555777"
variation 12
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461140321"
variation 13
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106623124"
variation 19
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:898157286"
variation 20
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349864418"
variation 22
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1226310238"
variation 29
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1286149706"
variation 36
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1004647109"
variation 38
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061552390"
variation 39
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:907286199"
variation 40
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1264877009"
variation 45
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061552338"
variation 47
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1201005244"
variation 50
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061552306"
variation 52
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1456841293"
variation 54
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:111647271"
misc_feature 57..59
/gene="TMEM40"
/note="upstream in-frame stop codon"
variation 57
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061552251"
variation 64
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489884384"
variation 65
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201757082"
exon 70..150
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 70
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:554298828"
variation 72
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1334089670"
variation 74
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:771747873"
variation 75
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:745880701"
variation 76
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:778681912"
variation 77
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756838370"
CDS 78..551
/gene="TMEM40"
/note="isoform d is encoded by transcript variant 4"
/codon_start=1
/product="transmembrane protein 40 isoform d"
/protein_id="NP_001271337.1"
/db_xref="CCDS:CCDS68347.1"
/db_xref="GeneID:55287"
/db_xref="HGNC:HGNC:25620"
/translation="
METSASSSQPQDNSQVHRETEDVDCPGHGEPDVLKDELQLYGDAPGEVVPSGESGLRRRGSDPASGEVEASQLRRLNIKKDDEFFHFVLLCFAIGALLVCYHYYADWFMSLGVGLLTFASLETVGIYFGLVYRIHSVLQGFIPLFQKFRLTGFRKTD"
misc_feature 186..545
/gene="TMEM40"
/note="Transmembrane protein 40 family; Region: TMEM40;
pfam15817"
/db_xref="CDD:464892"
variation 78
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378759603"
variation 79
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061459636"
variation 81
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177576409"
variation 82
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:534045803"
variation 84
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:753348848"
variation 85
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061459517"
variation 92
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1237774656"
variation 93..101
/gene="TMEM40"
/replace="tcctcc"
/replace="tcctcctcc"
/db_xref="dbSNP:2061459324"
variation 93
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755760542"
variation 94
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061459413"
variation 95
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:751985921"
variation 97
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376280227"
variation 101
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1181885301"
variation 103
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:763196102"
variation 104
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1352316279"
variation 105
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1306714694"
variation 106
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765614026"
variation 108
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213676333"
variation 109
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:373195760"
variation 113
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775983882"
variation 116
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1283926641"
variation 119
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776628023"
variation 122
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1464884197"
variation 123
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061458956"
variation 130
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1329112731"
variation 135
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:764317274"
variation 138
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1393426184"
variation 141
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061458839"
variation 142
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307710995"
variation 144
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760949908"
variation 146
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419244728"
variation 147
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775566858"
variation 149
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:771938508"
exon 151..204
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 151
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061391943"
variation 155
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751437669"
variation 156
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061391846"
variation 161
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:779680125"
variation 162..165
/gene="TMEM40"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1433016693"
variation 162
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:757813828"
variation 163
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:750136247"
variation 164
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391680924"
variation 165
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:764930665"
variation 167
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061391565"
variation 168
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1362468360"
variation 170
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061391503"
variation 173
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:75917614"
variation 174
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:544710139"
variation 178
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:774718081"
variation 182
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:147051806"
variation 183
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061391344"
variation 185
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1473646979"
variation 188
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:762921329"
variation 189
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446668104"
variation 190
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:369888905"
variation 191
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:769936195"
variation 193
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:747949810"
variation 194
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:147608337"
variation 195
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392339075"
variation 198
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:768433349"
variation 199
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047604956"
variation 202
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:747005245"
variation 203
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1380345955"
variation 204
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1575733961"
exon 205..240
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 210
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:760519202"
variation 213
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061356089"
variation 214
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061356063"
variation 217
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:201284102"
variation 218
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1376845516"
variation 220
/gene="TMEM40"
/replace=""
/replace="t"
/db_xref="dbSNP:1303447674"
variation 222
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:143024232"
variation 223
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367231631"
variation 225
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:759461512"
variation 230
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:774401744"
variation 233
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:34632635"
variation 240
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1303872903"
exon 241..273
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 241
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219116298"
variation 242
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061352003"
variation 246
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756191439"
variation 247
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:144017136"
variation 250
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:113852939"
variation 255
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061351805"
variation 256
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1044795477"
variation 262
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:777040204"
variation 263
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345878507"
variation 264
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:192420814"
variation 265
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:751333865"
variation 268
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354302728"
variation 269
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:201898990"
variation 272
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:763050250"
exon 274..321
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 275
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372524828"
variation 276
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:760390215"
variation 277
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:199973876"
variation 279
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:186695288"
variation 280
/gene="TMEM40"
/replace=""
/replace="t"
/db_xref="dbSNP:1559524365"
variation 281
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:749619163"
variation 282
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:935284406"
variation 285
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:370097007"
variation 286
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:770270888"
variation 287
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:748191325"
variation 292
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1262893957"
variation 297
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339511174"
variation 299..300
/gene="TMEM40"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2061348069"
variation 299
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1269040654"
variation 302
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224575860"
variation 305
/gene="TMEM40"
/replace=""
/replace="g"
/db_xref="dbSNP:1321915437"
variation 307
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:367768113"
variation 309
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334691432"
variation 310
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:58619724"
variation 314
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:58194358"
variation 315
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:755077473"
variation 316
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:747282610"
variation 318
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:923858021"
variation 319
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1333974661"
variation 321
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410976328"
exon 322..393
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 322
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:552698091"
variation 323
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1470355082"
variation 324
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:746059728"
variation 327
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:960173379"
variation 333
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:778831448"
variation 335
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1559523737"
variation 336
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061341758"
variation 338
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:759003406"
variation 339
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:201284335"
variation 341
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:777641656"
variation 344
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345326620"
variation 345
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287649219"
variation 347
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1368924026"
variation 348
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061341599"
variation 350
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:966066812"
variation 354
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:139984617"
variation 355
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:752136985"
variation 357
/gene="TMEM40"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1450788139"
variation 357
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:550278148"
variation 359
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356218473"
variation 360
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:759291365"
variation 362
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1412958493"
variation 364
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450480545"
variation 368
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314961568"
variation 371
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:751168020"
variation 372
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:953462561"
variation 384
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:776220889"
variation 385
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:762034501"
variation 387
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061341161"
variation 389
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:373401700"
variation 390
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760847101"
variation 391
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1418427179"
variation 393
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061341045"
exon 394..468
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 395
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1469130769"
variation 397
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061339983"
variation 399
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164164101"
variation 403
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273179654"
variation 406
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:759490002"
variation 408
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061339879"
variation 409
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061339858"
variation 410
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061339842"
variation 414
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:774670198"
variation 416
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:977553907"
variation 417
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:770995861"
variation 418
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:868310575"
variation 420
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061339693"
variation 422
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1488586319"
variation 423
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1360154395"
variation 424
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1276765886"
variation 425
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:749095466"
variation 427
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773049502"
variation 429
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1325197141"
variation 430
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:879899138"
variation 431
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:199796616"
variation 432
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:911874972"
variation 436
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:748125475"
variation 437
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061339409"
variation 439
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1453098809"
variation 446
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:975450770"
variation 447
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416950549"
variation 448
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:530184924"
variation 456
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455019771"
variation 457
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1252734807"
variation 458
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1245647594"
variation 461
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1019610401"
variation 462
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370473375"
variation 465
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756746842"
variation 468
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061339099"
exon 469..531
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 469
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253897426"
variation 470
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:573756207"
variation 474
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:142014087"
variation 475
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:778662525"
variation 476
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061331662"
variation 478
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:756581348"
variation 479
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1559522794"
variation 480
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:981186990"
variation 485
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:752942962"
variation 486
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:781731021"
variation 487
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061331426"
variation 494
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:755496353"
variation 496
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766488618"
variation 497
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106603947"
variation 501
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188760686"
variation 502
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038019158"
variation 503..507
/gene="TMEM40"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:774951652"
variation 503
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1004834801"
variation 504
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:763000143"
variation 506
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422589609"
variation 507
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:147042676"
variation 509
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061330989"
variation 513
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046382107"
variation 520
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061330927"
variation 523
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761682115"
variation 524
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1310290440"
variation 525
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1323328731"
variation 531
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:776346899"
exon 532..1797
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 533
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:78560646"
variation 537
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1575727833"
variation 538
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:572073706"
variation 540
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333571568"
variation 542..551
/gene="TMEM40"
/replace="gactga"
/replace="gactgactga"
/db_xref="dbSNP:771597719"
variation 546
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752057963"
variation 547
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1228908752"
variation 554
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:555363314"
variation 556
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:543359174"
variation 557
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:750443698"
variation 560
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:974451187"
variation 562
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061326186"
variation 563
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061326166"
variation 564
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1461347275"
variation 565
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:749797798"
variation 566
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061326110"
variation 567
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236830117"
variation 568
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:972914916"
variation 572
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:961590176"
variation 574
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462505977"
variation 577
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:370226089"
variation 583
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:762003898"
variation 584
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:754055798"
variation 586
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:763841790"
variation 587
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193984555"
variation 588
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1575727769"
variation 590
/gene="TMEM40"
/replace=""
/replace="t"
/db_xref="dbSNP:1559522311"
variation 590
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061325859"
variation 591
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430587953"
variation 596
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760466277"
variation 597
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287571324"
variation 599
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1197041325"
variation 600
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:11549481"
variation 602
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:187016181"
variation 603
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061325718"
variation 605..608
/gene="TMEM40"
/replace="cc"
/replace="cccc"
/db_xref="dbSNP:2061325646"
variation 606
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061325707"
variation 607
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281401864"
variation 608
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061325614"
variation 613
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061325591"
variation 615
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:373781796"
variation 616
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1376619076"
variation 617
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106603251"
variation 620
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:908947237"
variation 621
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061325505"
variation 622
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419424093"
variation 623
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005668509"
variation 627
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061325430"
variation 631
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1207397049"
variation 634
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061325382"
variation 643
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:895219593"
variation 644
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1382479847"
variation 645
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061325307"
variation 648
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1328805489"
variation 653
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061325266"
variation 655
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235878772"
variation 658
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1559522262"
variation 659
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:950546894"
variation 661
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:557354496"
variation 664
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061325139"
regulatory 666..671
/regulatory_class="polyA_signal_sequence"
/gene="TMEM40"
/note="hexamer: AATAAA"
variation 671
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106603194"
variation 673
/gene="TMEM40"
/replace=""
/replace="a"
/db_xref="dbSNP:1352903966"
variation 673
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061325077"
variation 674
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061325043"
variation 677
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214172689"
variation 678
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1024774414"
variation 680
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061324962"
variation 684
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061324930"
polyA_site 690
/gene="TMEM40"
/note="major polyA site"
variation 693
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:184140764"
variation 695
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061324895"
variation 696..698
/gene="TMEM40"
/replace="tct"
/replace="tctct"
/db_xref="dbSNP:2061324871"
variation 703
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1033645097"
variation 704
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205988113"
variation 707
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061324816"
variation 709
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106603141"
variation 712
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061324793"
variation 716
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221154942"
variation 717
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452608250"
variation 720
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195596186"
variation 721
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106603125"
variation 723
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1396146687"
variation 724
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:959301594"
variation 731
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061324659"
variation 739
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061324642"
variation 741
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:780495165"
variation 744
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061324616"
variation 745
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061324600"
variation 748
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1157342573"
variation 751
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:571742502"
variation 755
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1034068547"
variation 761
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1000861742"
variation 762
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1003465624"
variation 763
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:557830885"
variation 764
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045602569"
variation 768
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:945938402"
variation 770
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442380720"
variation 771
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061324427"
variation 772..773
/gene="TMEM40"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2061324407"
variation 775
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1575727623"
variation 776
/gene="TMEM40"
/replace="c"
/replace="cctc"
/db_xref="dbSNP:1009687494"
variation 779
/gene="TMEM40"
/replace=""
/replace="a"
/db_xref="dbSNP:2061324337"
variation 781
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1376043722"
variation 785
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1559522192"
variation 786
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237933502"
variation 787
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061324259"
variation 790..793
/gene="TMEM40"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:891266065"
variation 791
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061324240"
variation 792
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1308841891"
variation 800
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061324180"
variation 801
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243831377"
variation 804..807
/gene="TMEM40"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:1467318551"
variation 807
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:191951760"
variation 812
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1215617283"
variation 815
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:932864291"
variation 817
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1054690212"
variation 822
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061323968"
variation 824
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039052998"
variation 827
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419981592"
variation 833
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:769316546"
variation 838
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1415193203"
variation 840
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462750727"
variation 845
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:565749503"
variation 848
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061323845"
variation 851
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:908906225"
variation 858
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344078949"
variation 859
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323795"
variation 863
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:143263158"
variation 866
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323768"
variation 867
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1299772836"
variation 872
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061323725"
variation 877
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061323714"
variation 878
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061323695"
variation 884
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373970379"
variation 885
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323664"
variation 886
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061323619"
variation 891
/gene="TMEM40"
/replace=""
/replace="g"
/db_xref="dbSNP:763965908"
variation 891
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395176903"
variation 892
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323569"
variation 894
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:929062423"
variation 898
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323532"
variation 902
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1415788974"
variation 910
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323501"
variation 914
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:529252664"
variation 918
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1317334783"
variation 919
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061323445"
variation 921
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392931789"
variation 923
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323399"
variation 925
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:917726590"
variation 927
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106602915"
variation 928
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:758190414"
variation 929
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061323353"
variation 931
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1181636886"
variation 932
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:560203523"
variation 934
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:922245044"
variation 935
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:149560856"
variation 937
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422510477"
variation 942
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061323196"
variation 943
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1407645934"
variation 945
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1575727508"
variation 946
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:780747504"
variation 950
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1171918400"
variation 951
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:547822092"
variation 953
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:984657318"
variation 958..959
/gene="TMEM40"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2061323033"
variation 958
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323059"
variation 959
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:926543031"
variation 961..963
/gene="TMEM40"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2061322965"
variation 962
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:959456134"
variation 963
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:968067857"
variation 967
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212868549"
variation 969
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061322917"
variation 972
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1033696155"
variation 974
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106602865"
variation 975..982
/gene="TMEM40"
/replace="g"
/replace="gtccactg"
/db_xref="dbSNP:1210092586"
variation 977
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106602861"
variation 978
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061322867"
variation 979
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061322852"
variation 981
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1317715882"
variation 982
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279830733"
variation 987
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1009615712"
variation 989
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:756928391"
variation 990
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061322745"
variation 998
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229412617"
variation 1000
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:955457370"
variation 1002
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:765132159"
variation 1003
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187756958"
variation 1005
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061322641"
variation 1006
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106602819"
variation 1011
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212731913"
variation 1012
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1361234908"
variation 1013
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432119914"
variation 1018
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1029805112"
variation 1019
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1377205179"
variation 1020
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:906569375"
variation 1021
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:73022960"
variation 1024
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061322480"
variation 1030
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061322461"
variation 1038
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061322445"
variation 1039
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:777725325"
variation 1041
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:533201631"
variation 1046
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061322392"
variation 1047
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:564227282"
variation 1048
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061322351"
variation 1049
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061322324"
variation 1050
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2106602762"
variation 1055
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061322310"
variation 1056
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061322288"
variation 1057..1058
/gene="TMEM40"
/replace=""
/replace="c"
/db_xref="dbSNP:1449519344"
variation 1057
/gene="TMEM40"
/replace=""
/replace="a"
/db_xref="dbSNP:2061322120"
variation 1057
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010189712"
variation 1058..1065
/gene="TMEM40"
/replace="ttttttt"
/replace="tttttttt"
/replace="ttttttttt"
/db_xref="dbSNP:1233697830"
variation 1058
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061322027"
variation 1059
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1428936263"
variation 1061
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:900020982"
variation 1065
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321950"
variation 1067
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:758201843"
variation 1069
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006226627"
variation 1071
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061321873"
variation 1072..1080
/gene="TMEM40"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/replace="aaaaaaaaaa"
/db_xref="dbSNP:571290515"
variation 1072
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1054302206"
variation 1076
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047406760"
variation 1077
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1559521994"
variation 1078
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1168831260"
variation 1080
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061321736"
variation 1081..1082
/gene="TMEM40"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1487836902"
variation 1081
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2106602693"
variation 1082
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1559521975"
variation 1083
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321687"
variation 1085
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:917653039"
variation 1092
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1396800309"
variation 1095
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428422583"
variation 1099..1108
/gene="TMEM40"
/replace=""
/replace="agaaactaaa"
/db_xref="dbSNP:1559521952"
variation 1100
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1559521958"
variation 1103
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454709670"
variation 1104
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:935802110"
variation 1108
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415099851"
variation 1109
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056166540"
variation 1110
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061321528"
variation 1111
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:889555568"
variation 1112
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1575727366"
variation 1113
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1484692269"
variation 1116
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321452"
variation 1119
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256910426"
variation 1120
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321397"
variation 1121
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1324031836"
variation 1122
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321368"
variation 1123
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373817976"
variation 1124
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061321310"
variation 1126
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061321281"
variation 1127
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061321265"
variation 1129
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321238"
variation 1130
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049528363"
variation 1131
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:186721457"
variation 1136
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106602607"
variation 1137
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106602604"
variation 1141
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:922295826"
variation 1143
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:527348786"
variation 1145
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565286019"
variation 1146
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:940288964"
variation 1147
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1333778835"
variation 1152
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211274247"
variation 1158
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061321047"
variation 1159
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321028"
variation 1162
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254380179"
variation 1170
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:543891434"
variation 1172
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061320968"
variation 1173
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1177879766"
variation 1174
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:561743747"
variation 1175
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1313260472"
variation 1176
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061320883"
variation 1182
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061320867"
variation 1184
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:913879963"
variation 1187
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776127551"
variation 1190
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:182996297"
variation 1194
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061320772"
variation 1198
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061320762"
variation 1199
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:955385950"
variation 1200..1201
/gene="TMEM40"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2061320710"
variation 1203
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353008754"
variation 1205
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061320608"
variation 1206
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106602517"
variation 1207
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1162839130"
variation 1209
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396838472"
variation 1210
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1441758196"
variation 1213
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:575937892"
variation 1218
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328699630"
variation 1219..1223
/gene="TMEM40"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:2061320479"
variation 1220
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061320500"
variation 1223
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061320457"
variation 1224
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1334526865"
variation 1225
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444801147"
variation 1226
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1410027438"
variation 1227
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1372079483"
variation 1228
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:191855001"
variation 1233
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061320322"
variation 1234..1242
/gene="TMEM40"
/replace="tttttttt"
/replace="ttttttttt"
/replace="tttttttttt"
/db_xref="dbSNP:531847151"
variation 1242
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:982192029"
variation 1246
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061320259"
variation 1248
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334877087"
variation 1251
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061320231"
variation 1252
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061320214"
variation 1255
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:561509065"
variation 1256..1257
/gene="TMEM40"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1270725312"
variation 1257
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:970779301"
variation 1258
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1020995949"
variation 1259
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:138496707"
variation 1260..1280
/gene="TMEM40"
/replace="gtacatacctg"
/replace="gtacatacctgtacatacctg"
/db_xref="dbSNP:2061319859"
variation 1260
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061320105"
variation 1261
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256587958"
variation 1263
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:964211486"
variation 1264
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:955994532"
variation 1266
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1575727243"
variation 1268
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061320018"
variation 1269
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061319997"
variation 1272
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017525322"
variation 1273
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061319962"
variation 1274
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061319934"
variation 1275
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1033316141"
variation 1276
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1394966644"
variation 1277
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1167451441"
variation 1281
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1329939972"
variation 1282
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:577823696"
variation 1290
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360940403"
variation 1292
/gene="TMEM40"
/replace=""
/replace="a"
/db_xref="dbSNP:1417239478"
variation 1293
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355712069"
variation 1295
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061319664"
variation 1297
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1183035746"
variation 1302
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061319609"
variation 1307
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:368027790"
variation 1313
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:557894404"
variation 1314
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1196357619"
variation 1315
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049581794"
variation 1316
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047331885"
variation 1317
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1575727209"
variation 1320
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061319463"
variation 1321
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061319447"
variation 1322
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061319436"
variation 1324
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1484542768"
variation 1327
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:997973118"
variation 1332
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:900885350"
variation 1337
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1036709497"
variation 1342
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259862199"
variation 1345
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:939654196"
variation 1350
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061319299"
variation 1353
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192524021"
variation 1354
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1480155561"
variation 1356
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1371459537"
variation 1361
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061319222"
variation 1362
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061319205"
variation 1363
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061319185"
variation 1366
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265870515"
variation 1370
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1575727178"
variation 1372
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215482393"
variation 1373
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:201820100"
variation 1375
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061319092"
variation 1379
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:910154428"
variation 1381
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:111300148"
variation 1382
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:938255041"
variation 1384
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061319011"
variation 1385
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318994"
variation 1388
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318979"
variation 1389
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:374274432"
variation 1390
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375671511"
variation 1395
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061318932"
variation 1396
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:4684873"
variation 1399
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1304327322"
variation 1403
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1368726760"
variation 1405
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302519316"
variation 1408..1409
/gene="TMEM40"
/replace=""
/replace="tt"
/db_xref="dbSNP:1460309668"
variation 1408..1409
/gene="TMEM40"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1280835299"
variation 1408
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:79636268"
variation 1409..1411
/gene="TMEM40"
/replace=""
/replace="taa"
/db_xref="dbSNP:2106602292"
variation 1409..1410
/gene="TMEM40"
/replace=""
/replace="ta"
/db_xref="dbSNP:1394457233"
variation 1409
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1295719667"
variation 1410..1425
/gene="TMEM40"
/replace="aaaaaaaaaaa"
/replace="aaaaaaaaaaaa"
/replace="aaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaaaaaaa"
/db_xref="dbSNP:rs371416811"
variation 1410
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:75135909"
variation 1411
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:368364111"
variation 1414
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318623"
variation 1420..1421
/gene="TMEM40"
/replace=""
/replace="g"
/db_xref="dbSNP:2061318602"
variation 1422
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318586"
variation 1424
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318569"
variation 1425..1433
/gene="TMEM40"
/replace="a"
/replace="agacaaata"
/db_xref="dbSNP:2061318339"
variation 1426
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1575727122"
variation 1427
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318437"
variation 1428
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1575727119"
variation 1429..1435
/gene="TMEM40"
/replace="aaa"
/replace="aaataaa"
/db_xref="dbSNP:1175883619"
variation 1429..1431
/gene="TMEM40"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:1160580651"
variation 1432
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1453186639"
variation 1433
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106602238"
variation 1437
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318300"
variation 1440
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318284"
variation 1442
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378622935"
variation 1444
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171051062"
variation 1447
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061318218"
variation 1449
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1458849275"
variation 1454
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061318184"
variation 1455
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1453521549"
variation 1456
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1286712883"
variation 1457
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:937765087"
variation 1459
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061318019"
variation 1462
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:926828928"
variation 1464
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:904986395"
variation 1467
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061317963"
variation 1469
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061317946"
variation 1473
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061317931"
variation 1475
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368663796"
variation 1479
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061317890"
variation 1482
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1181348334"
variation 1486
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1304099712"
variation 1487
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1316076473"
variation 1490
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1434050554"
variation 1491
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043969277"
variation 1495
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259124259"
variation 1496
/gene="TMEM40"
/replace=""
/replace="t"
/db_xref="dbSNP:2061317745"
variation 1499
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1575727057"
variation 1502
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061317711"
variation 1503
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061317691"
variation 1504..1507
/gene="TMEM40"
/replace="at"
/replace="atat"
/db_xref="dbSNP:2061317638"
variation 1504
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353180640"
variation 1505
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:982244380"
variation 1507
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:970792316"
variation 1508
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:913804721"
variation 1512..1514
/gene="TMEM40"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2106602166"
variation 1518
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:988079636"
variation 1522
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:555427769"
variation 1524
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:750488799"
variation 1527
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:913944643"
variation 1528
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1418792913"
variation 1529
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1575727031"
variation 1534
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061317451"
variation 1537
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:922607566"
variation 1542
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061317416"
variation 1548
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061317382"
variation 1551
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:988175450"
variation 1552
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272434166"
variation 1556
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:113231678"
variation 1559
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:7626048"
variation 1560
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462592681"
variation 1562
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061317231"
variation 1563
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1000147868"
variation 1567
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061317196"
variation 1570
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1372544367"
variation 1571
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:879463121"
variation 1574
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061317145"
variation 1575
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:953940518"
variation 1582
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061317103"
variation 1584
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237868039"
variation 1587
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061317075"
variation 1589
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061317057"
variation 1590
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312447007"
variation 1595
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061317020"
variation 1597
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1306055461"
variation 1598
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061316971"
variation 1599
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439097537"
variation 1605
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229295581"
variation 1606
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017076554"
variation 1607
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1370756899"
variation 1611
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:369561840"
variation 1613
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106602090"
variation 1616
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061316834"
variation 1617
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1437975459"
variation 1620
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061316768"
variation 1623
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061316750"
variation 1625
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061316727"
variation 1626
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061316714"
variation 1629
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478672208"
variation 1630
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061316681"
variation 1640
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1382878591"
variation 1643
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1175819973"
variation 1646
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2106602064"
variation 1649..1650
/gene="TMEM40"
/replace="g"
/replace="gg"
/db_xref="dbSNP:549728818"
variation 1650
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1253170755"
variation 1653
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186731337"
variation 1654
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1415219866"
variation 1655
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028162612"
variation 1659
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1164931337"
variation 1665
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353852173"
variation 1672
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:997986150"
variation 1676
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061316474"
variation 1678
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061316452"
variation 1681
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1460439460"
variation 1686
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061316426"
variation 1687
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1379543055"
variation 1701
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:900934953"
variation 1702
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172045703"
variation 1703
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061316348"
variation 1705
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061316335"
variation 1711
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1452271734"
variation 1713
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037164895"
variation 1715
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1014495352"
variation 1717
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061316250"
variation 1723
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003948212"
variation 1729
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:896120426"
variation 1732
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:888141067"
variation 1733
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1048053338"
variation 1738
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253628195"
variation 1739
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061316116"
variation 1740
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061316096"
variation 1741
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:938307308"
variation 1744
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061316060"
variation 1750
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061316041"
variation 1751
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061316025"
variation 1757
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:905415695"
variation 1759
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1046560537"
variation 1769
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:949531026"
variation 1770
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1180890994"
variation 1771
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:904953560"
regulatory 1775..1780
/regulatory_class="polyA_signal_sequence"
/gene="TMEM40"
/note="hexamer: AATAAA"
variation 1781
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106601989"
variation 1784
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259015025"
variation 1793
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:377712522"
variation 1794
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:550052209"
polyA_site 1797
/gene="TMEM40"
/note="major polyA site"
ORIGIN
gaccagcccagcatccacatagtctacacagagctccccttgctgcccagacaagctgaaggaccacaggaaaagccatggagacttcagcatcctcctcccagcctcaggacaacagtcaagtccacagagaaacagaagatgtagactgtcctgggcatggggagcctgacgttttgaaggatgagcttcaactctatggagatgctcctggagaggtggtaccctctggggaatcaggactccgaaggagaggctctgacccagcaagtggagaagtggaggcctctcagttaagaagactgaatataaagaaagatgatgagtttttccatttcgtcctcctgtgctttgccatcggggccttgctggtgtgttatcactattacgcagactggttcatgtctcttggggtcggcctgctcaccttcgcctccctggaaaccgttggcatctacttcggactagtgtaccgtatccacagcgtcctccaaggcttcatccccctcttccagaagtttaggctgacagggttcaggaagactgactgaggccacttccaggtgggcagcagaggcaggccccagtgtgaccaccactgcgacccctgagcccacaagggcagagcagcattctgagagacgcacaggagaccaagccagaccaataaacagaacacttttccttccatgtggtctgaatgttggcaccagcccgggcaggggcatctcatttgggcagtactgctgtgcaacccagctgcaaggatggaaggcagagggtgggtgtggggcctgaggcttcacagtacctggaccagcaggaagattctgggaggtcactgctctcagaggacagcaagggaccctgagctctgcaagctgtgatctgtctgggttcatggtttttctcaaatcccaggctatctgcatgcgctctcaggtgctaccgagccatcctgggagagatggatggtccactgctttgaggcagggagccatcgggctggggccccttggtgaacctgatgcaggtaagatgctgaggactaaaaccattttttttgcacccaaaaaaaaaggcaggaaaatgatcatcagaaactaaatggcagccaggcatgggggctcacaactgtaatcctcgcactttgggaggctcaggctaagggtcgcttgaagctgagagttcaagaccaacctgggcaacatagtgagacccccatctctacaatttttttttaatgaccaaatgtggcggtacatacctgtacatacctgcggttccagctactcaagaggctgaggcaggaggactgcttgagcccaggagttcagggctgcagtgaggtacgatcaagccactgcactccagcctgggcgacagagcaagatcgtttctctaaaattaaaaaaaaaaaaaaaagacaaataaaaattgcatgtatttgtagtgtacaacatgttttgaaatatgtggaatggctaaatcaagctaattaacatatgtatccctcacataccctttttttatgatgagaacagtaaaaacctactgtcagcaatttgcaaagtatacaatacattgttattaactatggtcaccatgctatgtgattgatatcctgaacttgaactgagttcttgatggtcacagacatgctgttctcaaaactcagaagggtaacttctgaggttttgatttcaagtacttgtatgtaacctaatttaacgggagcccagagtgcacagatcagatatttattaaacatataaataaaacacagttttcacgata
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]